|
HS Code |
891284 |
| Chemical Name | 5-Nitrooxindole |
| Cas Number | 607-89-8 |
| Molecular Formula | C8H6N2O3 |
| Molecular Weight | 178.15 |
| Appearance | Yellow crystalline solid |
| Melting Point | 219-222°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry place; Keep container tightly closed |
| Synonyms | 5-Nitro-1,3-dihydro-2H-indol-2-one |
| Inchi | InChI=1S/C8H6N2O3/c11-8-6-3-5(10(12)13)1-2-7(6)9-4-8/h1-3,9H,4H2 |
| Smiles | C1C(=O)NC2=CC=C(C=C21)[N+](=O)[O-] |
As an accredited 5-Nitrooxindole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 5-Nitrooxindole, 25g, sealed in an amber glass bottle with tamper-evident cap, labeled with hazard symbols and product details. |
| Shipping | 5-Nitrooxindole is shipped in tightly sealed containers, compliant with chemical safety regulations. Packaging ensures protection from moisture, light, and mechanical damage. The substance is labeled as hazardous, with appropriate handling and transport documentation provided. Shipments follow applicable local and international guidelines for the safe transport of laboratory chemicals. |
| Storage | 5-Nitrooxindole should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from sources of ignition, heat, and direct sunlight. It should be kept away from incompatible substances such as strong oxidizing agents. Proper labeling and secondary containment are recommended to prevent accidental release. Use only in chemical fume hoods or approved laboratory environments. |
Applications of 5-Nitrooxindole in Industrial ManufacturingWe supply 5-Nitrooxindole at scale for integration into demanding industrial processes. Below, we detail its practical roles across select, verifiable sectors, outlining regulatory alignment, formulation ratios, process deployment, and end-use product context. 1. Pharmaceutical Intermediates for Anticancer Compound SynthesisPharmaceutical manufacturers incorporate 5-Nitrooxindole into key steps for synthesizing intermediate molecules found in targeted anticancer agents. The nitro and oxindole moieties facilitate ring-closure and aromatic substitution in application-specific multi-step synthesis. Operators control feedstock purity and reactivity to prevent by-product formation and adhere to defined impurity thresholds during these transformations, enabling downstream conversion to quinoline or indole derivatives used in ongoing drug development pipelines. Industry compliance standards
Typical usage ratio
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2. Agrochemical Synthesis Building BlocksAgrochemical formulators employ 5-Nitrooxindole in the stepwise construction of bioactive heterocyclic scaffolds present in crop-protection agents, particularly in insecticide and herbicide candidate libraries. The electron-deficient nitro group serves as a key functional handle for subsequent functionalization, supporting pericyclic reactions and allowing the introduction of further substituents needed for field efficacy while minimizing off-target toxicity during product stewardship review. Industry compliance standards
Typical usage ratio
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3. Dye and Pigment Intermediate ManufacturingTextile and specialty dye manufacturers use 5-Nitrooxindole as a controlled introduction point for nitro functional groups in the synthesis of high-performance chromophore intermediates. It participates in ring-opening and reductive coupling reactions, influencing color intensity and brilliance. Technicians monitor purity and functional group availability to prevent batch color drifts and comply with quality audits demanded by global dye customers, while integrating it with compatible solvents approved for colorant applications. Industry compliance standards
Typical usage ratio
Downstream process integration
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4. Research Reagents for Chemical BiologyResearch institutions and fine chemical producers apply 5-Nitrooxindole to generate specific labeling reagents and probes aimed at studying nitroaromatic metabolism and protein-ligand interactions. Chemists value its reactivity profile for selective incorporation in chemical probes and conjugation with biomolecules or metal catalysts under well-defined, controlled laboratory conditions. Consistency and trace impurity management are critical for reproducibility in published results and for downstream bioconjugate synthesis. Industry compliance standards
Typical usage ratio
Downstream process integration
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This compound, known by its chemical family as 5-Nitrooxindole, isn’t just a niche organic intermediate. Over years in chemical manufacturing, we’ve watched this tiny yellow solid show up in more places than many would expect—fields that stretch from advanced pharmaceutical development to specialty agrochemical approaches, to the slow, careful work of new materials research. Every time a researcher or production chemist calls about 5-Nitrooxindole, the conversation gets practical quickly. They don’t want just another catalog chemical. They need predictable performance, truthful quality, a product born of attentive batch control and direct oversight.
Our connection to this molecule begins before the reaction flask even heats up. We've designed our process around precision, starting with containment and handling of isatin—careful, deliberate dosing ensures the nitro substitution runs to completion and leaves minimal byproducts. In our facility, we've implemented a fine-tuned crystallization regimen: solvents are matched to temperature and purity targets, filtration pressures are adjusted by operators—never just left to autopilot. Every kilogram has a batch log and in-house analytical checks—HPLC, NMR, and basic spectroscopy run in tight sequence before packaging. We don’t leave the fate of our product to unmonitored machines: a laboratory professional, with basic senses as well as analytical data, puts eyes on the final goods. This method sets us apart from bulk processors who chase volume over carefulness.
Our 5-Nitrooxindole model balances convenience for scaled-up users and consistency for R&D chemists. The purity consistently sits at 98% or better by HPLC and quantitative NMR—year after year. No customer has ever seen an out-of-spec batch leave our floor; that’s practical discipline, not a slogan. The particle size steps out of a mill that's checked every shift for retention and screen shape. You won’t find rocks, dust, or the frustrating clumping common to material shipped across several hands. The odor, color, and flow match our published profile—pale yellow, free-flowing, almost no scent—which often tells returning customers they’re looking at material we prepared, not a blend or repackage.
You’ve probably noticed that many “suppliers” online claim a vast catalog of oxindole derivatives but aren’t hands-on with real chemistry. That gap appears in their shipments: unexpected solvents, inconsistent yields, and peak impurities. Such surprises are more than paperwork headaches. In drug discovery, a single impurity can throw off SAR studies or patent claims; in pigment precursors, an off-color can ruin production quality. Every kilogram of 5-Nitrooxindole made in our plant travels one step: cradle to customer. No third-party repack, no shadow batch from a mystery partner. Our own chemists can give specifics about batch date, lot composition, and any deviation, because we’re present in the room making process decisions daily.
Unlike big volume intermediates where price rules every aspect, 5-Nitrooxindole trades on traceability and consistency—nuclear magnetic resonance showing a clean aromatic region, UV-visible scans aligning with reference spectra, confirmed melting points always within our documented window. Not many supply chain links let a buyer speak with the QC chemist, or track back to the technician who weighed and labeled the sample. Here, it’s not just allowed—it’s expected by returning partners.
Over time, we’ve watched 5-Nitrooxindole find its way into a surprising range of end uses. Medicinal chemists reach for it as a building block when tweaking lead compounds—its oxindole core accepts further alkylation or coupling, and the nitro group directs electronic effects in downstream cyclizations. It’s not just theory: over two dozen peer-reviewed syntheses from the past decade name this molecule as a key intermediate en route to kinase inhibitors, antiviral scaffolds, and several exploratory oncology projects. Structure-activity teams choose this substance because it’s neither too reactive nor too inert; you actually get a working conversion under standard conditions.
On the colorant side, new pigment chemistries with improved UV performance sometimes build around the oxindole motif. We’ve seen clients take our 5-Nitrooxindole shipments, transform them via reduction or condensation, and print digital textile colors with shades not possible ten years ago. Some agricultural projects look for this intermediate as a stepping stone to modified indoles—compounds with regulatory scrutiny and evolving application profiles. Here, a repeatable, verified starting material can mean the difference between regulatory approval and failure, since batch-to-batch analytical “noise” is strictly limited.
Direct control is more than product identity or basic assay values. Our quality assurance doesn’t take holiday breaks. We confirm each batch against a reference spectrum generated in our own lab. If the UV cut-off or nitro peak slips, someone pulls the batch card and starts again. We know our customers run parallel analyses—no one enjoys guessing whether a product’s main impurity sits at 0.5% or 2%—and our business depends on their confidence. Few resellers can trace a product’s journey from raw material receipt to tamper-evident seal like we do in our operations.
We handle shipment in a direct line—unbroken custody from final package to departure. Most orders head out in high-barrier, moisture-shielded containers, since oxindole derivatives show some sensitivity to atmospheric moisture if left loosely packaged. It’s not a formality; even a few hours in an open drum can let trace hydrolysis begin, changing the purity or forming hard-to-remove residues. Customers who run old inventory or partial batches see the benefit, as our packaging shows less clumping or strange residue than other lots they’ve handled.
We support direct communication. You can expect that a single email reaches both our sales coordinator and the lab where your batch currently sits. If questions arise—unusual solubility, analytical anomaly, or practical concern about a new method—we answer with specifics, drawn from firsthand runs. A trader can repeat a COA line or PDF; only a manufacturer living with the chemistry can offer root-cause guidance.
Plant operators deal with the realities of nitro chemistry and can offer guidance. For instance, minimizing dust during transfer prevents cross-contamination. 5-Nitrooxindole shows lower volatility than some related compounds, but airborne particulate during drum changeover remains a risk. That’s handled with standard negative pressure and designated transfer areas. These control measures cut down both loss and the slow, cumulative operator exposure that large-scale handling can bring.
We’ve tuned our synthetic route to avoid using chlorinated solvents at scale except during downstream washing or fine purification. While alternate synthesis routes pop up in literature, many hinge on harder-to-control oxidants, higher costs, or unreliable conversion. That’s a lesson learned through batches that underperformed or showed obscured exotherms during scale-up. Customers end up receiving a cleaner, more reproducible material that behaves as expected whether their batch requires gram, multi-kilogram, or even ton-scale supplies. We believe those process choices speak to accountability, not just cost-saving.
Waste minimization is part of our operation. Nitrofuran byproducts and mother liquor residuals don’t simply get sent for bulk incineration. Instead, they’re monitored, collected, and processed through our on-site solvent recovery and managed transition metals capture. We know environmental responsibility demands more than symbolic gestures. Auditors have visited our facility and walked through waste handling—so our word carries the weight of real observation, not just claims.
Pharmaceutical users often ask about impurity carry-through. Our in-house experience shows most extraneous peaks come from incomplete nitration or trace side reactions from the parent isatin. These can look minor on a basic TLC but rise on full LC-MS. If you’re running downstream cross-coupling or metal-catalyzed steps, residual halides or nitrated byproducts can foul up catalyst cycles. We include full impurity profiles—acquired in-house, never relayed from a generalized database—so project timelines stay on track. Pre-purchase conversations with project chemists have led us to make modest tweaks to grind size or final wash pH for specific customers. We know the value of saving a high-value intermediate from a late-stage QC failure.
For pigments and specialty chemical buyers, solubility and color tone take center stage. Our technical staff runs routine comparative dissolution and colorimetry checks. Years ago, we had a pigment user report a brownish tint in a drum’s contents. That batch was reviewed and matched against reference; minor photo-degradation was found. Since then, we’ve revamped storage to include full-spectrum lighting limits and UV-blocking drums. Real user feedback lessens issues over time.
We maintain direct, traceable lines back to each raw material in our production chain. No batch goes dark in between steps. We log materials, batch times, operator checkpoints, and in-process testing. This sort of data backbone pays dividends for both regulatory confidence and user trust. Customers in regulated industries count on that transparency, and researchers running novel syntheses appreciate being able to trace a surprise impurity to its source—rather than down a rabbit hole of guesswork and supplier runaround.
Technical data sheets rarely capture the questions that arrive from real users. Handbooks don’t answer: which solvent best dissolves 5-Nitrooxindole for scale-up? What’s the decomposition profile under high-shear granulation? Over years of direct production and customer inquiry, our team has built a working knowledge base. We know successful recrystallization often prefers an ethyl acetate–hexane gradient rather than pure organic. Short-path vac drying protects from over-drying and caking—particularly in high-humidity climates. Such tips, built from factory experiments, shave days or even weeks off development cycles for our industrial partners.
Our lab bridges languages between high-level researchers and production technologists. Routine calls include requests for batch-specific COAs, complete chromatographic data, and even first-hand observations of flow and storage behavior. A researcher with a bottlenecked route, or a formulator trying to meet unusual granulation specs, gets live advice from a chemist who’s made the compound, not just sold it. That’s a promise we can uphold because of the way we operate—closer to chemistry and end use, farther from generic commodity trading.
Dependable supply means little without quality that tracks from order to order. Each batch of 5-Nitrooxindole comes stamped not just with a lot number, but an untold history of checks and careful handling. Operators oversee raw feed weighing, document every step, troubleshoot unexpected color shifts, and step in whenever batch data falls outside spec. Our production routine has been shaped by both repeated success and rare stumbles—each points toward tighter oversight, better feedback, and incremental improvements.
For buyers who have juggled erratic shipments, incomplete paperwork, or analytical mismatches, our model answers those frustrations with blunt accountability. No shipment leaves without a second set of lab checks, full documentation, and a readiness to support follow-up questions. Users in regulated or high-spec industries routinely audit our facility, walking the same production floor as our shift workers; that level of openness reflects a genuine commitment, not just a market differentiator.
The challenge isn’t just about delivering a compound meeting specs. It’s about earning authority through consistent, repeated, and transparent manufacturing. That edge doesn’t come through price alone or through ad copy. It comes from a working relationship with both the chemistry and the user base. Each order tells us something new—a question about shelf stability, advice on single-step derivatization, a tweak that helps one user avoid a workup bottleneck the next time around.
Our history with 5-Nitrooxindole began with requests for an obscure intermediate. Each batch since then sharpened our skills, closing the gap between theory and practical delivery. Today’s product stands on rigorous process control and an open channel to our user base. We don’t separate manufacturing from technical support—they grow together with every new order, every bit of feedback looped back into the line.
We invite practical questions, technical scrutiny, and honest dialogue about 5-Nitrooxindole. The product ships with integrity because the hands that make it take pride in every lot. No shortcut or third-party anonymity—just grounded manufacturing shaped by years of direct experience, and a belief that quality claims aren’t just earned, they’re proven in every shipment, every analysis, and every conversation with our customers. That’s not just a difference—it’s the definition of what we deliver in every drum and every partnership.